10 years of experience in
鈥� Vaccines manufacturing and development.
鈥� Deviation Investigation
鈥� Process robustness improvement ,control and Process Performance Tracking,
鈥� Scale up and Technology transfer
鈥� Validation and Qualification
鈥� Responsible for online manufacturing behavior by step by step trending
鈥� Responsible to do timely investigation if any trend fluctuations observed in process for
instant process improvements.
鈥� Preparation of SOPs, BPRs, MFRs, and IQ, OQ and PQ of critical process instruments and equipments.Handling of QMS activities Deviations, failure investigation, CAPA and Change control management
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